HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586987Generated: October 30, 2026
Trifluoroacetic acid → HCID 9981209, compound
https://huagongshe.com/reaction/1586987
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | O-Benzylhydroxylamine | HCID 102313 | — |
| Reactant | HCID 10315565 | HCID 10315565 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 9981209 | HCID 9981209 | 61% |
Reaction Steps
Trifluoroacetic acid (16.6 g) was added in one portion to a solution of 5,6,7,8-tetrahydro-5-hydroxy-2-(phenylmethoxy)-5-(phenylmethyl)quinoline (50 g), phenylmethoxyamine (44.8 g), and toluene (600 ml) at room temperature. The solution was stirred at room temperature for 19 hrs, and the reaction mixture was quenched with conc ammonium hydroxide solution. The layers were separated and the aqueous phase was extracted with ethyl acetate. The combined organic layers were washed with brine, dried over potassium carbonate, filtered, and the filtrate was concentrated. Purification by high performance liquid chromatography (silica gel, elution with ethyl acetate-hexanes) gave 40.0 g (61% of 5,6,7,8-tetrahydro-N,2-bis(phenylmethoxy)-5-(phenylmethyl)-5-quinolinamine
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05216164 |
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| Source dataset | uspto-grants-1993_06 |
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| ORD ID | ord-915d42b933ff4ceea2e4d3c881559f0f |
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| Source note | uspto-grants-1993_06 |
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